المؤلفون: Baudin P; Sorbonne Université, Paris Brain Institute - Institut du Cerveau, ICM, INSERM, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France., Cousyn L; Sorbonne Université, Paris Brain Institute - Institut du Cerveau, ICM, INSERM, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.; AP-HP, Epilepsy Unit, Pitié-Salpêtrière Hospital, DMU Neurosciences, Paris, France., Navarro V; Sorbonne Université, Paris Brain Institute - Institut du Cerveau, ICM, INSERM, CNRS, AP-HP, Pitié-Salpêtrière Hospital, Paris, France. vincent.navarro@aphp.fr.; AP-HP, Epilepsy Unit, Pitié-Salpêtrière Hospital, DMU Neurosciences, Paris, France. vincent.navarro@aphp.fr.; AP-HP, Center of Reference for Rare Epilepsies, Pitié-Salpêtrière Hospital, 47-83 Boulevard de l'Hôpital, 75013, Paris, France. vincent.navarro@aphp.fr.

المصدر: Cellular and molecular life sciences : CMLS [Cell Mol Life Sci] 2021 Dec 30; Vol. 79 (1), pp. 16. Date of Electronic Publication: 2021 Dec 30.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Springer Country of Publication: Switzerland NLM ID: 9705402 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-9071 (Electronic) Linking ISSN: 1420682X NLM ISO Abbreviation: Cell Mol Life Sci Subsets: MEDLINE

مواضيع طبية MeSH: Intracellular Signaling Peptides and Proteins/*chemistry , Intracellular Signaling Peptides and Proteins/*genetics , Mutation/*genetics , Seizures/*genetics , Seizures/*physiopathology, Animals ; Humans ; Intracellular Signaling Peptides and Proteins/metabolism ; Models, Biological ; Seizures/diagnostic imaging ; Synapses/metabolism

المؤلفون: Araki K; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan., Nakamura R; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan., Ito D; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan., Kato K; Department of Genetics, Research Institute of Environmental Medicine (RIEM), Nagoya University Graduate School of Medicine, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan., Iguchi Y; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan., Sahashi K; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan., Toyama M; Department of Genetics, Research Institute of Environmental Medicine (RIEM), Nagoya University Graduate School of Medicine, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan., Hamada K; Department of Neurology, Kamiiida Daiichi General Hospital, 2-70 Kamiiida-kitamachi, Kita-ku, Nagoya, 462-0802, Japan., Okamoto N; Department of Molecular Medicine, Research Institute, Osaka Women's and Children's Hospital, 840, Murodo-cho, Izumi, Osaka, 594-1101, Japan., Wada Y; Department of Molecular Medicine, Research Institute, Osaka Women's and Children's Hospital, 840, Murodo-cho, Izumi, Osaka, 594-1101, Japan., Nakamura T; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan; Department of Laboratory Medicine, Nagoya University Hospital, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan., Ogi T; Department of Genetics, Research Institute of Environmental Medicine (RIEM), Nagoya University Graduate School of Medicine, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan., Katsuno M; Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan. Electronic address: ka2no@med.nagoya-u.ac.jp.

المصدر: Epilepsy research [Epilepsy Res] 2020 Aug; Vol. 164, pp. 106371. Date of Electronic Publication: 2020 May 22.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Science Publishers Country of Publication: Netherlands NLM ID: 8703089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-6844 (Electronic) Linking ISSN: 09201211 NLM ISO Abbreviation: Epilepsy Res Subsets: MEDLINE

مواضيع طبية MeSH: Cerebellar Ataxia/*genetics , Epilepsy, Absence/*genetics , Mutation/*genetics , Receptors, Cell Surface/*genetics , Tremor/*genetics, Epilepsy, Generalized/genetics ; Female ; Heterozygote ; Humans ; Male ; Pedigree

المؤلفون: Garcia-Gomes MSA; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil. Electronic address: mari-aranha@usp.br., Zanatto DA; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil., Galvis-Alonso OY; Department of Molecular Biology, Medicine School of São José do Rio Preto (FAMERP), Brazil., Mejia J; Hospital Israelita Albert Einstein, São Paulo, Brazil., Antiorio ATFB; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil., Yamamoto PK; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil., Olivato MCM; Federal University of São Paulo (UNIFESP), Brazil., Sandini TM; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil., Flório JC; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil., Lebrun I; Laboratory of Biochemistry and Biophysics, Butantan Institute, Brazil., Massironi SMG; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil; Department of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), Brazil., Alexandre-Ribeiro SR; Department of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), Brazil., Bernardi MM; Paulista University, Brazil., Ienne S; Core Facility for Scientific Research - University of São Paulo (CEFAP-USP/GENIAL (Genome Investigation and Analysis Laboratory), Brazil., de Souza TA; Department of Microbiology, Institute of Biomedical Science, University of São Paulo (USP), Brazil., Dagli MLZ; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil., Mori CMC; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Brazil.

المصدر: Epilepsy & behavior : E&B [Epilepsy Behav] 2020 Apr; Vol. 105, pp. 106945. Date of Electronic Publication: 2020 Feb 25.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 100892858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-5069 (Electronic) Linking ISSN: 15255050 NLM ISO Abbreviation: Epilepsy Behav Subsets: MEDLINE

مواضيع طبية MeSH: Acoustic Stimulation/*adverse effects , Epilepsy, Reflex/*genetics , Epilepsy, Reflex/*metabolism , Mutation/*genetics , Tremor/*genetics , Tremor/*metabolism, Animals ; Disease Models, Animal ; Dopamine/metabolism ; Female ; Glutamic Acid/metabolism ; Hippocampus/chemistry ; Hippocampus/metabolism ; Male ; Mice ; Mice, Transgenic ; Norepinephrine/metabolism ; Seizures/genetics ; Seizures/metabolism ; Serotonin/metabolism

المؤلفون: Bernardo P; Department of Paediatric Neurosciences, Santobono-Pausilipon Children's Hospital, Naples, Department of Translational Medical Sciences, Child and Adolescent Neuropsychiatry, University of Naples Federico II, Naples., Ferretti A; NESMOS Department, Sant' Andrea Hospital, 'Sapienza' University of Rome, Rome., Terrone G; Department of Translational Medical Sciences, Child and Adolescent Neuropsychiatry, University of Naples Federico II, Naples., Santoro C; Regional Referral Centre for Neurofibromatosis, Department of Woman, Child, General and Specialistic Surgery, 'Luigi Vanvitelli' University of Naples, Naples., Bravaccio C; Department of Translational Medical Sciences, Child and Adolescent Neuropsychiatry, University of Naples Federico II, Naples., Striano S; Department of Neuroscience, Reproductive and Odontostomatological Sciences, Epilepsy Centre, Federico II University, Naples., Coppola A; Department of Neuroscience, Reproductive and Odontostomatological Sciences, Epilepsy Centre, Federico II University, Naples., Striano P; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto 'G. Gaslini', Genova.

المصدر: Epileptic disorders : international epilepsy journal with videotape [Epileptic Disord] 2019 Jun 01; Vol. 21 (3), pp. 271-277.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 100891853 Publication Model: Print Cited Medium: Internet ISSN: 1950-6945 (Electronic) Linking ISSN: 12949361 NLM ISO Abbreviation: Epileptic Disord Subsets: MEDLINE

مواضيع طبية MeSH: Epilepsy/*therapy , Mutation/*genetics , Protein Serine-Threonine Kinases/*genetics , Spasms, Infantile/*genetics, Child ; Electroencephalography/methods ; Epilepsy/genetics ; Epileptic Syndromes/diagnosis ; Epileptic Syndromes/genetics ; Epileptic Syndromes/therapy ; Female ; Humans ; Phenotype ; Rett Syndrome/genetics ; Seizures/genetics ; Spasms, Infantile/diagnosis ; Spasms, Infantile/therapy

SCR Disease Name: CDKL5 deficiency disorder; Infantile Epileptic-Dyskinetic Encephalopathy

المؤلفون: Myers KA; Research Institute of the McGill University Health Center, 2155 Guy Street, Montreal, PQ, H3H 2L9, Canada; Department of Pediatrics, Division of Child Neurology, Montreal Children's Hospital, McGill University Health Centre, 1001 Boulevard Décarie, Montreal, PQ, H4A 3J1, Canada. Electronic address: kenneth.myers@mcgill.ca., Shevell MI; Research Institute of the McGill University Health Center, 2155 Guy Street, Montreal, PQ, H3H 2L9, Canada; Department of Pediatrics, Division of Child Neurology, Montreal Children's Hospital, McGill University Health Centre, 1001 Boulevard Décarie, Montreal, PQ, H4A 3J1, Canada., Sébire G; Research Institute of the McGill University Health Center, 2155 Guy Street, Montreal, PQ, H3H 2L9, Canada; Department of Pediatrics, Division of Child Neurology, Montreal Children's Hospital, McGill University Health Centre, 1001 Boulevard Décarie, Montreal, PQ, H4A 3J1, Canada.

المصدر: Epilepsy research [Epilepsy Res] 2019 Feb; Vol. 150, pp. 66-69. Date of Electronic Publication: 2019 Jan 14.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Science Publishers Country of Publication: Netherlands NLM ID: 8703089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-6844 (Electronic) Linking ISSN: 09201211 NLM ISO Abbreviation: Epilepsy Res Subsets: MEDLINE

مواضيع طبية MeSH: Death, Sudden*, Epilepsy/*genetics , Epilepsy/*physiopathology , Mutation/*genetics , NAV1.1 Voltage-Gated Sodium Channel/*genetics , Voltage-Gated Sodium Channel beta-1 Subunit/*genetics, Adolescent ; Adult ; Child ; Family Health ; Female ; Genetic Testing ; Humans ; Infant ; Male ; Middle Aged

المؤلفون: Richards KL; Ion Channels and Disease Group, Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia., Milligan CJ; Ion Channels and Disease Group, Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia., Richardson RJ; Ion Channels and Disease Group, Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia., Jancovski N; Ion Channels and Disease Group, Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia., Grunnet M; Neuroscience Drug Discovery, H. Lundbeck A/S, DK-2500 Valby, Denmark.; Department of Drug Design and Pharmacology, Copenhagen University, DK-2100 Copenhagen, Denmark., Jacobson LH; Sleep and Cognition Group, Epilepsy Division, Florey Insitute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia.; Department of Pharmacology and Therapeutics, The University of Melbourne, Parkville, VIC 3010, Australia., Undheim EAB; Centre for Advanced Imaging, The University of Queensland, Brisbane, QLD 4072, Australia., Mobli M; Centre for Advanced Imaging, The University of Queensland, Brisbane, QLD 4072, Australia., Chow CY; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia., Herzig V; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia., Csoti A; Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Panyi G; Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Reid CA; Ion Channels and Disease Group, Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia.; Department of Medicine, The University of Melbourne, Parkville, VIC 3010, Australia., King GF; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; glenn.king@imb.uq.edu.au spetrou@unimelb.edu.au., Petrou S; Ion Channels and Disease Group, Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia; glenn.king@imb.uq.edu.au spetrou@unimelb.edu.au.; Department of Medicine, The University of Melbourne, Parkville, VIC 3010, Australia.

المصدر: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2018 Aug 21; Vol. 115 (34), pp. E8077-E8085. Date of Electronic Publication: 2018 Aug 03.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1091-6490 (Electronic) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, Epilepsies, Myoclonic/*drug therapy , Interneurons/*metabolism , NAV1.1 Voltage-Gated Sodium Channel/*metabolism , Spider Venoms/*pharmacology , Synaptic Transmission/*drug effects, Animals ; CHO Cells ; Cricetulus ; Epilepsies, Myoclonic/genetics ; Epilepsies, Myoclonic/metabolism ; Epilepsies, Myoclonic/pathology ; HEK293 Cells ; Humans ; Interneurons/pathology ; Mice ; Mice, Mutant Strains ; NAV1.1 Voltage-Gated Sodium Channel/genetics

المؤلفون: Liu XW; Department of Neurology, Qilu Hospital of Shandong University, China., Li W; Department of Neurology, Qilu Hospital of Shandong University, China. Electronic address: sjnklwn@163.com., Han T; Department of Neurology, Qilu Hospital of Shandong University, China., Wei K; Department of Neurology, Qilu Hospital of Shandong University, China., Qiao S; Department of Neurology, Qilu Hospital of Shandong University, China., Su L; Department of Neurology, Qilu Hospital of Shandong University, China., Chi Z; Department of Neurology, Qilu Hospital of Shandong University, China.

المصدر: Clinical neurology and neurosurgery [Clin Neurol Neurosurg] 2018 Jun; Vol. 169, pp. 86-91. Date of Electronic Publication: 2017 Nov 04.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 7502039 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-6968 (Electronic) Linking ISSN: 03038467 NLM ISO Abbreviation: Clin Neurol Neurosurg Subsets: MEDLINE

مواضيع طبية MeSH: Epilepsy, Generalized/*genetics , Mutation/*genetics , NAV1.2 Voltage-Gated Sodium Channel/*genetics , Seizures, Febrile/*genetics , Twins, Monozygotic/*genetics , Exome Sequencing/*methods, Amino Acid Sequence ; Child, Preschool ; Epilepsy, Generalized/diagnosis ; Heterozygote ; Humans ; Male ; Seizures, Febrile/diagnosis

المؤلفون: Jiang YL; Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China., Yuan F; Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China., Yang Y; Shaanxi Institute of Pediatric Diseases, Xi'an Children's Hospital, Xi'an, China., Sun XL; Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China., Song L; Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China., Jiang W; Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China. Electronic address: jiangwen@fmmu.edu.cn.

المصدر: Seizure [Seizure] 2018 Mar; Vol. 56, pp. 88-91. Date of Electronic Publication: 2018 Feb 10.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: England NLM ID: 9306979 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2688 (Electronic) Linking ISSN: 10591311 NLM ISO Abbreviation: Seizure Subsets: MEDLINE

مواضيع طبية MeSH: Dystonia/*complications , Dystonia/*genetics , Mutation/*genetics , Receptors, Nicotinic/*genetics , Seizures, Febrile/*complications , Seizures, Febrile/*genetics, Adolescent ; Child ; DNA Mutational Analysis ; Family Health ; Female ; Humans ; Male

SCR Disease Name: Familial paroxysmal dystonia

المؤلفون: Bernardo P; Department of Mental Health, Physical and Preventive Medicine, Clinic of Child and Adolescent Neuropsychiatry, University of Campania 'Luigi Vanvitelli', Naples, Italy. Electronic address: pia.bernardo84@gmail.com., Galletta D; Section of Psychiatry Unit on Treatment Resistant Psychosis, and Laboratory of Molecular and Translational Psychiatry, Department of Neuroscience, University School of Medicine Federico II, Naples, Italy. Electronic address: diana.galletta@unina.it., Iasevoli F; Section of Psychiatry Unit on Treatment Resistant Psychosis, and Laboratory of Molecular and Translational Psychiatry, Department of Neuroscience, University School of Medicine Federico II, Naples, Italy. Electronic address: felix_ias@hotmail.com., D'Ambrosio L; Section of Psychiatry Unit on Treatment Resistant Psychosis, and Laboratory of Molecular and Translational Psychiatry, Department of Neuroscience, University School of Medicine Federico II, Naples, Italy. Electronic address: luigidambrosio@hotmail.it., Troisi S; Department of Neuroscience, Reproductive and Odontostomatological Sciences, Epilepsy Centre, Federico II University, Naples, Italy. Electronic address: serena.troisi@gmail.com., Gennaro E; Genetic Laboratory, E.O. Ospedali Galliera, Genova, Italy. Electronic address: elena.gennaro@galliera.it., Zara F; Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 'G. Gaslini' Institute, Genoa, Italy. Electronic address: federicozara@ospedale-gaslini.ge.it., Striano S; Department of Neuroscience, Reproductive and Odontostomatological Sciences, Epilepsy Centre, Federico II University, Naples, Italy. Electronic address: sstriano1@gmail.com., de Bartolomeis A; Section of Psychiatry Unit on Treatment Resistant Psychosis, and Laboratory of Molecular and Translational Psychiatry, Department of Neuroscience, University School of Medicine Federico II, Naples, Italy. Electronic address: adebarto@unina.it., Coppola A; Department of Neuroscience, Reproductive and Odontostomatological Sciences, Epilepsy Centre, Federico II University, Naples, Italy. Electronic address: antonietta.coppola1@gmail.com.

المصدر: Seizure [Seizure] 2017 Oct; Vol. 51, pp. 186-189. Date of Electronic Publication: 2017 Sep 06.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: England NLM ID: 9306979 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2688 (Electronic) Linking ISSN: 10591311 NLM ISO Abbreviation: Seizure Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, DNA-Binding Proteins/*genetics , Epilepsy/*genetics , Intellectual Disability/*genetics, Adult ; Epilepsy/pathology ; Epilepsy/physiopathology ; Epilepsy/psychology ; Female ; Humans ; Intellectual Disability/pathology ; Intellectual Disability/physiopathology ; Phenotype ; Psychotic Disorders/genetics ; Psychotic Disorders/pathology ; Psychotic Disorders/physiopathology

المؤلفون: Hur YJ; Epilepsy Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL; Department of Pediatrics, Haeundae Paik Hospital, Inje University College of Medicine, Pusan, Republic of Korea., Koh S; Epilepsy Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL; Department of Pediatrics, Children's Healthcare of Atlanta, Emory University, Atlanta, GA., Millichap J; Epilepsy Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL., Nangia S; Epilepsy Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL., Jennings LJ; Epilepsy Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL., Nordli DR Jr; Epilepsy Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL; Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, CA. Electronic address: dnordli@chla.usc.edu.

المصدر: The Journal of pediatrics [J Pediatr] 2017 May; Vol. 184, pp. 172-177.e1. Date of Electronic Publication: 2017 Mar 02.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Mosby Country of Publication: United States NLM ID: 0375410 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-6833 (Electronic) Linking ISSN: 00223476 NLM ISO Abbreviation: J Pediatr Subsets: MEDLINE

مواضيع طبية MeSH: Electroencephalography* , Mutation*, Epilepsy/*diagnostic imaging , Epilepsy/*genetics, Female ; Humans ; Infant ; Male ; Retrospective Studies